Structure of PDB 1bfd Chain A Binding Site BS03
Receptor Information
>1bfd Chain A (length=523) Species:
303
(Pseudomonas putida) [
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ASVHGTTYELLRRQGIDTVFGNPGSNELPFLKDFPEDFRYILALQEACVV
GIADGYAQASRKPAFINLHSAAGTGNAMGALSNAWNSHSPLIVTAGQQTR
AMIGVEALLTNVDAANLPRPLVKWSYEPASAAEVPHAMSRAIHMASMAPQ
GPVYLSVPYDDWDKDADPQSHHLFDRHVSSSVRLNDQDLDILVKALNSAS
NPAIVLGPDVDAANANADCVMLAERLKAPVWVAPSAPRCPFPTRHPCFRG
LMPAGIAAISQLLEGHDVVLVIGAPVFRYHQYDPGQYLKPGTRLISVTCD
PLEAARAPMGDAIVADIGAMASALANLVEESSRQLPTAAPEPAKVDQDAG
RLHPETVFDTLNDMAPENAIYLNESTSTTAQMWQRLNMRNPGSYYFCAAG
GLGFALPAAIGVQLAEPERQVIAVIGDGSANYSISALWTAAQYNIPTIFV
IMNNGTYGALRWFAGVLEAENVPGLDVPGIDFRALAKGYGVQALKADNLE
QLKGSLQEALSAKGPVLIEVSTV
Ligand information
Ligand ID
TPP
InChI
InChI=1S/C12H18N4O7P2S/c1-8-11(3-4-22-25(20,21)23-24(17,18)19)26-7-16(8)6-10-5-14-9(2)15-12(10)13/h5,7H,3-4,6H2,1-2H3,(H4-,13,14,15,17,18,19,20,21)/p+1
InChIKey
AYEKOFBPNLCAJY-UHFFFAOYSA-O
SMILES
Software
SMILES
CACTVS 3.341
Cc1ncc(C[n+]2csc(CCO[P@@](O)(=O)O[P](O)(O)=O)c2C)c(N)n1
OpenEye OEToolkits 1.5.0
Cc1c(sc[n+]1Cc2cnc(nc2N)C)CCO[P@](=O)(O)OP(=O)(O)O
OpenEye OEToolkits 1.5.0
Cc1c(sc[n+]1Cc2cnc(nc2N)C)CCOP(=O)(O)OP(=O)(O)O
CACTVS 3.341
Cc1ncc(C[n+]2csc(CCO[P](O)(=O)O[P](O)(O)=O)c2C)c(N)n1
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCCc1sc[n+](c1C)Cc2c(nc(nc2)C)N
Formula
C12 H19 N4 O7 P2 S
Name
THIAMINE DIPHOSPHATE
ChEMBL
CHEMBL1236376
DrugBank
ZINC
ZINC000008215517
PDB chain
1bfd Chain A Residue 530 [
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Receptor-Ligand Complex Structure
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PDB
1bfd
The crystal structure of benzoylformate decarboxylase at 1.6 A resolution: diversity of catalytic residues in thiamin diphosphate-dependent enzymes.
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
T377 S378 L403 G427 D428 G429 S430 Y433 T457 Y458 G459 A460 L461
Binding residue
(residue number reindexed from 1)
T376 S377 L402 G426 D427 G428 S429 Y432 T456 Y457 G458 A459 L460
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
N23 G25 S26 N27 E28 E47 H70 L109 L110 T111 N112 Y160 P254 H281 S376 G401 L403 D428 N455 T457 Y458 A460 L461 F464
Catalytic site (residue number reindexed from 1)
N22 G24 S25 N26 E27 E46 H69 L108 L109 T110 N111 Y159 P253 H280 S375 G400 L402 D427 N454 T456 Y457 A459 L460 F463
Enzyme Commision number
4.1.1.7
: benzoylformate decarboxylase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0003984
acetolactate synthase activity
GO:0016831
carboxy-lyase activity
GO:0030976
thiamine pyrophosphate binding
GO:0046872
metal ion binding
GO:0050660
flavin adenine dinucleotide binding
GO:0050695
benzoylformate decarboxylase activity
Biological Process
GO:0009056
catabolic process
GO:0018924
mandelate metabolic process
GO:0019596
mandelate catabolic process
GO:0019752
carboxylic acid metabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1bfd
,
PDBe:1bfd
,
PDBj:1bfd
PDBsum
1bfd
PubMed
9665697
UniProt
P20906
|MDLC_PSEPU Benzoylformate decarboxylase (Gene Name=mdlC)
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